US4132669AExpiredUtility

Process for preparing phosphorous-alumina catalysts using polycarboxylic acids as extrusion aids

Assignee: NALCO CHEMICAL COPriority: Oct 6, 1977Filed: Oct 6, 1977Granted: Jan 2, 1979
Est. expiryOct 6, 1997(expired)· nominal 20-yr term from priority
B01J 27/16B01J 37/0009
60
PatentIndex Score
15
Cited by
5
References
6
Claims

Abstract

Alumina-phosphorous powders can be extruded into catalysts supports having improved properties by the addition of up to 15% by weight of a polycarboxylic acid, containing 2-10 carbon atoms, based on the dry weight of the alumina-phosphorous powder prior to extrusion. The addition of the polycarboxylic acid also increases the extrusion rate.

Claims

exact text as granted — not AI-modified
We claim: 
     
       1. A process for preparing phospha-alumina extrudates having a relatively high crush strength, and relatively reduced pore volume in pores above 600 A diameter comprising: A. preparing a purified phospha-alumina powder comprising on a dry basis 3-30% P 2  O 5  and 70-97% Al 2  O 3 .   B. mixing said purified phospha-alumina powder with water and from 0.1-15% by weight of a water-soluble polycarboxylic acid containing from 1-10 carbon atoms based on the dry weight of the powder.   C. adjusting the moisture content of said phospha-alumina powder to an extrudate level so as to allow extrusion; and then,   D. extruding said phospha-alumina powder to prepare a phospha-alumina extrudate whereby the extrusion rate is improved over phospha-alumina powders not so treated.   
     
     
       2. The process of claim 1 where the polycarboxylic acid is citric acid. 
     
     
       3. The process of claim 1 wherein the phospha-alumina extrudate is dried and calcined to prepare a catalyst support. 
     
     
       4. The process of claim 1 where the crush strength is increased by at least 25% over non-polycarboxylic acid treated material. 
     
     
       5. The process of claim 1 where pore volume above 600 A of the product is decreased relative to that where no polycarboxylic acid is used. 
     
     
       6. The process of claim 1 where the shrinkage on calcination is increased over that where no polycarboxylic acid is used.

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